4.8 Article

Direct Detection of Reactive Gallium-Hydride Species on the Ga2O3 Surface via Solid-State NMR Spectroscopy

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AMER CHEMICAL SOC
DOI: 10.1021/jacs.2c01005

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资金

  1. National Key R&D Program of China [2021YFA1502803]
  2. National Natural Science Foundation of China [21773230, 91945302, 21902158]
  3. LiaoNing Revitalization Talents Program [XLYC1807207]
  4. China National Postdoctoral Program for Innovative Talents [BX20190321]
  5. China Postdoctoral Science Foundation [2019M651154]
  6. BP P.L.C.
  7. DICPQIBEBT [UN201808]
  8. DICP [I202104]

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This study reports the first direct and unambiguous NMR evidence of highly reactive surface gallium hydrides (Ga-H) over a practical Ga(2)O(3) catalyst during H2 activation. The spectroscopic effects of different isotopes of Ga on the 1H NMR signal are distinguished, allowing for the discrimination of Ga-H signal from other groups. The analysis also reveals the role of Ga-H species in catalytic reactions and provides insights for designing more efficient Ga-based catalysts.
Surface metal hydrides (M-H) are ubiquitous in heterogeneous catalytic reactions, while the detailed characterizations are frequently hindered by their high reactivity/low concentration, and the complicated surface structures of the host solids, especially in terms of practical solid catalysts. Herein, combining instant quenching capture and advanced solid-state NMR methodology, we report the first direct and unambiguous NMR evidence on the highly reactive surface gallium hydrides (Ga-H) over a practical Ga(2)O(3 )catalyst during direct H2 activation. The spectroscopic effects of 69Ga and 71Ga isotopes on the 1H NMR signal are clearly differentiated and clarified, allowing a concrete discrimination of the Ga-H signal from the hydroxyl crowd. Accompanied with quantitative and two-dimensional NMR spectroscopical methods, as well as density functional theory calculations, information on the site specification, structural configuration, and formation mechanism of the Ga-H species has been revealed, along with the H2 dissociation mechanism. More importantly, the successful spectroscopic identification and isolation of the surface Ga-H allow us to clearly reveal the critical but ubiquitous intermediate role of this species in catalytic reactions, such as propane dehydrogenation and CO2 hydrogenation reactions. The analytic approach presented in this work can be extended to other M-H analysis, and the insights will benefit the design of more efficient Ga-based catalysts.

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